Rosenberg J C, Lysz K
Transplantation. 1978 Mar;25(3):115-20. doi: 10.1097/00007890-197803000-00004.
In order to gain insight into the immunosuppresive mechanism of action of corticosteroids, an in vitro model of the cellular immune response was used to study the effect of methylprednisolone on human lymphocyte-mediated cytotoxicity. Concentrations from 0.25 to 10 microgram/ml were equally effective in producing 74% suppression lymphocyte-mediated cytotoxicity when the steroid was present during the entire period of in vitro sensitization. A 12.5-fold increase in effector to target cell ratio was required to achieve 30% 51Cr release when cytotoxic lymphocytes were generated in the prescence of methylprednisolone. Lymphocyte-mediated cytotoxicity was suppressed 48% when methylprednisolone was present only during the initial 24 hr of the 7-day in vitro sensitization period. Methylprednisolone also effectively inhibited cytotoxicity when it was incubated with sensitized lymphocytes for 3hr before incubating these cells with target cells. Our observations suggest that two of the major immunosuppressive mechanisms of action methylprednisolone are suppression of the generation of cytotoxic lymphocytes and suppression of specifically sensitized cytotoxic lymphocytes.
为深入了解皮质类固醇的免疫抑制作用机制,采用细胞免疫反应的体外模型研究甲泼尼龙对人淋巴细胞介导的细胞毒性的影响。当在体外致敏的整个期间存在类固醇时,浓度为0.25至10微克/毫升在产生74%抑制淋巴细胞介导的细胞毒性方面同样有效。当在甲泼尼龙存在下产生细胞毒性淋巴细胞时,效应细胞与靶细胞的比例需要增加12.5倍才能达到30%的51Cr释放。当甲泼尼龙仅在7天体外致敏期的最初24小时存在时,淋巴细胞介导的细胞毒性被抑制48%。在将致敏淋巴细胞与靶细胞孵育前,甲泼尼龙与致敏淋巴细胞孵育3小时也能有效抑制细胞毒性。我们的观察结果表明,甲泼尼龙的两个主要免疫抑制作用机制是抑制细胞毒性淋巴细胞的产生和抑制特异性致敏的细胞毒性淋巴细胞。